Laboratoire D'ingénierie Des protéines Et Des molécules Bioactives, Université de Carthage, INSAT, Centre urbain nord, BP 676, 1080, Cedex Tunis, Tunisia.
Next Generation Processes and Products, NGP², RWTH Aachen University, Forckenbeckstr. 51, 52074, Aachen, Germany.
World J Microbiol Biotechnol. 2019 Dec 12;36(1):5. doi: 10.1007/s11274-019-2779-6.
Stranded green macroalgae represents an important and renewable biomass that remains under valorized despite the numerous environmental problems generated by their accumulation in coastal regions. This work describes the isolation of a filamentous thermophile fungus identified as Aspergillus terreus JL1 that produces an efficient cellulolytic activity for green macroalgae saccharification. The characterization of the endoglucanase activity obtained after submerged fermentation showed a differential induction depending on the carbon source used with a unique isoform released when Ulva lactuca was used as inducer. The crude extract obtained hydrolyzed efficiently the untreated algal biomass (70.5%) compared to other cellulolytic extracts. The unique endoglucanase released was then purified to homogeneity (Yield: 49.6%; Specific activity: 30.1 U/mg; Purification fold: 4.36) and characterized biochemically. Its peptidic sequence was then determined and showed its belonging to the GH12. The described enzyme represents a promising biotechnological tool for algal biomass conversion.
搁浅的绿藻是一种重要的可再生生物质资源,尽管它们在沿海地区的大量积累会产生许多环境问题,但仍未得到充分利用。本工作描述了一种丝状嗜热真菌的分离,该真菌被鉴定为 Aspergillus terreus JL1,它对绿藻糖化具有高效的纤维素酶活性。经过深层发酵得到的内切葡聚糖酶活性的表征表明,其诱导取决于所使用的碳源,当使用 Ulva lactuca 作为诱导剂时,会释放出一种独特的同工酶。与其他纤维素酶提取物相比,从粗提物中获得的酶能够有效地水解未经处理的藻类生物质(70.5%)。然后,将释放出的独特内切葡聚糖酶纯化至均一性(产率:49.6%;比活性:30.1 U/mg;纯化倍数:4.36)并进行了生化特性表征。其肽序列随后被确定,并表明其属于 GH12。该酶代表了一种有前途的藻类生物质转化生物技术工具。